{"id":3795677,"url":"https://alion.io/job/icon-pharmacovigilance-supervisor","title":"Pharmacovigilance Supervisor","company":{"id":5677,"name":"ICON","domain":"iconplc.com","url":"https://alion.io/company/icon","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"A","score":85,"open_postings":58,"ghost_share":0,"stale_share":0.81,"repost_share":0,"time_to_fill_p50_days":20,"computed_at":"2026-11-06T05:58:05Z"}},"role":"Biotech","role_family":"Biotech","seniority":null,"employment_type":"full_time","work_mode":"remote","remote_scope":"stated_countries","remote_scope_basis":"board_field","remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Mexico City, Mexico"],"countries":["MX"],"hiring_countries":["MX"],"hiring_countries_total":1,"salary":null,"salary_estimate":null,"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[],"status":"live","first_seen_at":"2026-11-04T00:00:00Z","employer_posted_date":"2026-11-04","last_verified_at":"2026-11-06T06:27:57Z","board_verified":true,"closed_at":null,"days_open":2,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":2},"description":"Home Based - CDMX - Exp. People LeadAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.\nAs the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.\nAs a Supervisor, Pharmacovigilance at ICON, you will oversee the safety monitoring and reporting of adverse events related to clinical trials and marketed products.\nWhat You Will Do:\nYou will manage day-to-day pharmacovigilance and drug safety activities, supporting your team to deliver quality outcomes.\nKey responsibilities include:\nSupervising the day-to-day pharmacovigilance operations, ensuring timely and accurate reporting of adverse events.\nCollaborating with cross-functional teams, including clinical operations and regulatory affairs, to optimize pharmacovigilance processes.\nEnsuring compliance with global regulatory requirements and internal standard operating procedures for safety reporting.\nManaging safety data collection, analysis, and submission to regulatory authorities.\nProviding leadership and training to the pharmacovigilance team, ensuring adherence to best practices in safety monitoring.\nYour Profile:\nYou will have solid pharmacovigilance and drug safety experience, with the ability to manage competing priorities and develop your team.\nRequired qualifications and experience:\nBachelor's degree in life sciences, pharmacy, or a related field.\nExperience in pharmacovigilance or drug safety, with a focus on clinical trials or post-marketing surveillance.\nStrong knowledge of global pharmacovigilance regulations and guidelines.\nExcellent communication, leadership, and organizational skills, with the ability to manage a team effectively.\nDetail-oriented with the ability to manage multiple tasks and ensure accuracy in safety reporting.\nEmployment with ICON is contingent upon having the legal right to work in the country where the role is based.\nRewards & Benefits\nICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.\nBenefits may include:\nCompetitive base salary and performance related incentives\nHealth and wellbeing programmes including medical, dental, and vision coverage where applicable\nRetirement and pension plans\nLife assurance and disability coverage\nEmployee assistance programmes and wellbeing resources\nLearning and development opportunities through structured training and career pathways\nBenefits may vary depending on role and location.\nVisit our careers site to read more about the benefits ICON offers.\nInclusion and Accessibility\nICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.\nIf you require reasonable accommodations during the recruitment process, please let us know or submit a request here.\nAre you a current ICON Employee? 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